Association of specific p53 polymorphisms with keratosis in individuals exposed to arsenic through drinking water in West Bengal, India

被引:26
作者
De Chaudhuri, Sujata
Mahata, Julie
Das, Jayanta K.
Mukherjee, Angshuman
Ghosh, Papiya
Sau, Tanmoy Jyoti
Mondal, Lakshmikanta
Basu, Santanu
Giri, Ashok K.
Roychoudhury, Susanta
机构
[1] Indian Inst Chem Biol, Mol & Human Genet Div, Kolkata 700032, W Bengal, India
[2] W Bank Hosp, Dept Dermatol, Howrah 711109, India
[3] Vivekananda Inst Med Sci, Dept Neurol, Kolkata 700026, W Bengal, India
[4] Peerless Hosp, Kolkata 700009, W Bengal, India
[5] BK Roy Res Ctr, Kolkata 700009, W Bengal, India
[6] Calcutta Natl Med Coll, Dept Med, Kolkata 700014, W Bengal, India
[7] Calcutta Med Coll, Reg Inst Ophthalmol, Kolkata 700073, W Bengal, India
[8] Sri Aurobindo Seva Kendra, Dept Gen Med, Kolkata 700068, W Bengal, India
关键词
arsenic; p53; polymorphisms; codon; 72; keratosis;
D O I
10.1016/j.mrfmmm.2006.06.014
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Although, more than six million people are endemically exposed to inorganic arsenic in West Bengal, India by drinking heavily contaminated groundwater, only about 300,000 people show arsenic induced skin lesions. This suggests that genetic variability plays an important role in arsenic induced skin lesions and skin cancers. Arsenic induced keratosis is considered as a possible precancerous state of in situ carcinoma. Several reports have suggested the role of p53 polymorphisms as potential marker for risk assessment of different types of cancers. This prompted us to study the association of three p53 polymorphisms with arsenic induced keratosis in a population exposed to arsenic through drinking water. A total of 366 unrelated individuals (177 individuals with arsenic induced keratosis and 189 individuals with no arsenic induced skin lesions) were recruited from North 24 Parganas, Nadia and Murshidabad districts between January 2003 and February 2005 for the study of the genotypic distribution of three p53 polymorphisms (16 bp duplication at intron 3, codon 72 Arg/Pro and G > A at intron 6 [nt 13,494]) by PCR-RFLP. The arginine homozygous genotype at codon 72, and homozygous genotype of no duplication polymorphism at intron 3 were over represented in the individuals with keratosis compared with individuals with no skin lesions (OR = 2.086; 95% CI = 1.318-3.299 and OR = 2.086; 95% CI = 1.257-3.457, respectively). This study indicates that individuals carrying the arginine homozygous genotype at codon 72, and/or no duplication homozygous genotype at intron 3 are at risk for the development of arsenic induced keratosis. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:102 / 112
页数:11
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